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Terminated

NeoMedix Trabectome I/A Console, Model Number 550014, surgical aspirator

FDA Recall Z-0071-2008 · Posted 2008-09-29

Recalling FirmNeomedix Corp
Recall StatusTerminated
Product CodeBTA
Date Initiated2007-05-28
Date Terminated2008-09-29
Product Quantity7

Reason for Recall

Failure of irrigation flow: The pinch valve in a few pumps may not consistently open to allow irrigation flow. In over 450 surgeries, the firm confirmed one instance of a valve that did not open. The electrically activated pinch valve in the NeoMedix Trabectome I/A pump activates irrigation flow to the eye during Trabectome surgery.

Firm Action

On May 31, 2007 NeoMedix mailed a Customer letter to all consignees informing them of the hazard. The letter also indicated to the customers they NeoMedix has developed a minor modification/upgrade that is designed to assure that the pinch valve opens at the appropriate time. The customers were instructed this modification requires return of their existing pump for modification and testing at the firm's facility before its return. In the event that surgeries have already been scheduled, NeoMedix will provide a loaner unit until the suspect unit can be modified and returned to you. The letter also indicated the cost of the modification and/or use of a loaner unit will be entirely at NeoMedix expense. You will be contacted to establish the details of implementing this modification.

Root Cause

Nonconforming Material/Component

Distribution Pattern

Nationwide to: CA, HI, IA, NY & PA

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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